Senior Clinical Project Manager - CNS
New
J
JobgetherClinical research
Fully remote US-basedFull-TimeSenior
Salary not disclosed
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Job Details
- Languages
- Strong written and verbal communication skills with professional English proficiency.
- Experience
- At least 3 years of relevant clinical research industry experience.
- Required Skills
- Project ManagementMicrosoft Office
Requirements
- Bachelor’s degree, RN qualification, or equivalent combination of education, training, and relevant experience.
- At least 3 years of relevant clinical research industry experience.
- Clinical Project Manager experience appropriate to the level of responsibility required for successful study management.
- Supervisory experience and demonstrated ability to coordinate and guide project teams.
- Advanced knowledge of Good Clinical Practice, ICH guidelines, FDA requirements, and other applicable clinical research regulations.
- Intermediate knowledge of project management principles, methodologies, and techniques.
- Proficiency with Microsoft Office, Adobe, and project management software.
- Strong organizational and interpersonal skills for working across management levels and with internal and external stakeholders.
- Strong client service skills and ability to build credibility, maintain trust, and foster productive professional relationships.
- Ability to work independently and contribute effectively in a fast-paced team environment.
- Strong written and verbal communication skills with professional English proficiency.
- Strong attention to detail and ability to manage multiple priorities across complex clinical projects.
- Willingness and ability to travel approximately 10–20%.
Responsibilities
- Lead clinical studies through initiation, planning, execution, and closeout while managing timelines, budgets, scope, and quality.
- Coordinate cross-functional project teams and allocate resources to balance workloads.
- Lead client-facing project meetings, prepare agendas, document decisions, and maintain stakeholder communication.
- Develop and maintain Project Management Plans, Communication Plans, risk logs, timelines, milestone trackers, and project records.
- Manage study budgets, proposals, contracts, out-of-scope activities, financial tracking, and invoicing.
- Support study start-up by collecting confidentiality agreements, feasibility information, budgets, and clinical trial agreements.
- Maintain regulatory and study files, and oversee Trial Master File organization, accuracy, completeness, and inspection readiness.
- Identify risks, delays, and operational challenges and implement contingency and risk-control measures.
- Manage vendors and monitor their deliverables against study requirements, timelines, and quality expectations.
- Coordinate clinical reports and other study documentation, and ensure teams follow SOPs, GCP, ICH guidelines, applicable regulations, and study-specific training requirements.
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